organic chemistry, Eschenmoser's salt (named for Albert Eschenmoser) is the ionic, organic compound [(CH3)2NCH2]I. It is the iodide salt of the dimethylaminomethylene...

history of organic chemistry. The Eschenmoser fragmentation, the Eschenmoser sulfide contraction and Eschenmoser's salt are named after him. A particularly...

prenyl bromide, allyl bromide, propiolic acid, Gilman reagent, and Eschenmoser's salt. The taxol synthesis started from the terpene verbenone 1 in Scheme...

"Eschenmoser's salt" is a well known example of an iminium salt....

eventually hydrolyzes to give formyl. It is a source of "O=CH+". Eschenmoser's salt, [(CH3)2NCH2]I Paul R. Giles; Charles M. Marson (2001)....

Pirmasens), cancer. Albert Eschenmoser, 97, Swiss organic chemist (Eschenmoser's salt, Eschenmoser fragmentation, Eschenmoser sulfide contraction). Luís...

form a γ,δ-unsaturated amide. This was developed by Albert Eschenmoser in 1964. Eschenmoser-Claisen rearrangement was used as a key step in the total synthesis...

feature tertiary amines. Often they are obtained by alkylation with Eschenmoser's salt, a source of [CH2=N(CH3)2]+. A cobalt(III) complex of aminomethyl...

practiced in ethoxylation. Aminomethylation is often effected with Eschenmoser's salt, [(CH3)2NCH2]OTf John Hooz; Jorge Cabezas; Sergio Musmanni; Jose Calzada...

as a bidentate ligand. N,N,N′,N′-Tetramethylformamidinium chloride Eschenmoser's salt is used for similar applications. Gaudry, Michel; Jasor, Yves; Khac...